Evidence map›Paper›PMID 41723252›Full record

ArticleScientific reports2026

Effects of leonurine supplementation during in vitro culture on oxidative stress, cell proliferation, apoptosis, and autophagy in bovine embryos.

Hasan Alkan, Fatma Satilmis, Yunus Emre Deniz, Gonca Sonmez, Muhammed Hudai Culha, Muhammed Furkan Ciftci, Harun Yonar, Elif Tugba Bilim Kaya, Bahar Eda Goren, Omer Faruk Yesilkaya and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Hasan Alkan *Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Selcuk University, Alaeddin Keykubat Campus, Istanbul Street, Konya, 42003, Turkey. hasanalkan@selcuk.edu.tr.
Fatma Satilmis *Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Selcuk University, Alaeddin Keykubat Campus, Istanbul Street, Konya, 42003, Turkey.
Yunus Emre DenizDepartment of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Selcuk University, Alaeddin Keykubat Campus, Istanbul Street, Konya, 42003, Turkey.
Gonca SonmezDepartment of Genetics, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Muhammed Hudai CulhaDepartment of Genetics, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Muhammed Furkan CiftciDepartment of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Selcuk University, Alaeddin Keykubat Campus, Istanbul Street, Konya, 42003, Turkey.
Harun YonarDepartment of Biostatistics, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Elif Tugba Bilim KayaDepartment of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Selcuk University, Alaeddin Keykubat Campus, Istanbul Street, Konya, 42003, Turkey.
Bahar Eda GorenDepartment of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Selcuk University, Alaeddin Keykubat Campus, Istanbul Street, Konya, 42003, Turkey.
Omer Faruk YesilkayaDepartment of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Selcuk University, Alaeddin Keykubat Campus, Istanbul Street, Konya, 42003, Turkey.
Sıdıka SanDepartment of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Selcuk University, Alaeddin Keykubat Campus, Istanbul Street, Konya, 42003, Turkey.
Muhammed Ali DonmezDepartment of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Selcuk University, Alaeddin Keykubat Campus, Istanbul Street, Konya, 42003, Turkey.
Kubra Karakas Alkan *Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Selcuk University, Alaeddin Keykubat Campus, Istanbul Street, Konya, 42003, Turkey.

Funding

Selçuk University Research Foundation 23401109Türkiye Bilimsel ve Teknolojik Araştırma Kurumu 124O204
6 · The paper itself

Abstract

A critical factor contributing to the reduced production and development of embryos during in vitro production is oxidative stress, which arises due to excessive accumulation of reactive oxygen species (ROS). In order to reduce or prevent ROS levels in the culture medium and embryos, the use of antioxidant agents is commonplace. The present study sets out to evaluate the effects of leonurine, a compound with antioxidant properties, when supplemented into the in vitro culture medium, on embryo development and quality, cell proliferation, apoptosis, autophagy, ROS and GSH levels. Blastocyst quality was evaluated by performing differential staining, ROS, GSH, TUNEL, EdU, and LC3B staining on the developing embryos. The results demonstrated that the supplementation of the culture medium with 20 µM leonurine (Leo20) resulted in a significant enhancement of blastocyst development, as evidenced by increased numbers of ICM, TE, and TCC in embryos when compared to the control group. Furthermore, the number of apoptotic cells and the apoptotic index were found to be lower in the Leo20 group than in the control group. Furthermore, the levels of ROS and LC3B were reduced, while GSH levels were elevated in the leonurine-treated group. With regard to cell proliferation, the number of EdU-positive cells and the proliferation rate were found to be significantly higher in the Leo20 group than in the control group. Gene expression analysis revealed upregulation of antioxidant-related genes (SOD, GPX4, and CAT) and pluripotency-related genes (OCT4, NANOG, and SOX2), while the expression of apoptosis-related genes (BAX and CASP3) and autophagy-related genes (ATG12 and LC3B) was downregulated. It has been demonstrated that the supplementation of leonurine to an in vitro culture medium has the potential to enhance the efficiency of blastocyst formation and to improve the viability of embryos, a phenomenon that may be attributed to the ability of leonurine to reduce oxidative stress. Consequently, the reduction of oxidative stress in embryos is hypothesized to result in increased cell proliferation and decreased rates of apoptosis and autophagy.

Indexed as

ApoptosisAutophagyCell ProliferationEmbryo, MammalianGallic AcidOxidative StressAnimalsAntioxidantsBlastocystCattleCulture MediaEmbryo Culture TechniquesEmbryonic DevelopmentGlutathioneReactive Oxygen SpeciesAntioxidantsCulture MediaGallic AcidGlutathioneleonurineReactive Oxygen SpeciesAntioxidantBovineEmbryonic developmentIn vitro embryo productionLeonurine

Identifiers

PMID41723252
PMCPMC13022331

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.